Canonical Allele Identifier: CA340728605

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724428G>C (hg19) ; chr1:g.67258745G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258745G>C , CM000663.2:g.67258745G>C	GRCh38
NC_000001.10:g.67724428G>C , CM000663.1:g.67724428G>C	GRCh37
NC_000001.9:g.67497016G>C	NCBI36
NG_011498.1:g.97260G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1346G>C	ENSP00000513138.1:n.1346G>C
ENST00000697150.1:c.1404G>C	ENSP00000513139.1:n.1404G>C
ENST00000697151.1:c.1337G>C	ENSP00000513140.1:n.1337G>C
ENST00000697164.1:c.1417G>C	ENSP00000513153.1:p.Glu473Gln
ENST00000697165.1:c.1204G>C	ENSP00000513154.1:p.Glu402Gln
ENST00000347310.10:c.1507G>C MANE Select	ENSP00000321345.5:p.Glu503Gln
ENST00000637002.1:c.898G>C	ENSP00000490340.1:p.Glu300Gln
ENST00000347310.9:c.1507G>C	ENSP00000321345.5:p.Glu503Gln
ENST00000395227.2:c.301G>C	ENSP00000378652.2:p.Glu101Gln
ENST00000425614.3:c.742G>C	ENSP00000387640.2:p.Glu248Gln
ENST00000473881.2:c.*333G>C	ENSP00000486667.1:n.*333G>C
NM_144701.2:c.1507G>C	NP_653302.2:p.Glu503Gln
XM_005270516.2:c.745G>C	XP_005270573.1:p.Glu249Gln
XM_011540789.1:c.1597G>C	XP_011539091.1:p.Glu533Gln
XM_011540790.1:c.1507G>C	XP_011539092.1:p.Glu503Gln
XM_011540791.1:c.1507G>C	XP_011539093.1:p.Glu503Gln
XM_011540790.3:c.1507G>C	XP_011539092.1:p.Glu503Gln
XM_011540791.3:c.1507G>C	XP_011539093.1:p.Glu503Gln
XR_001736993.1:n.1587G>C
NM_144701.3:c.1507G>C MANE Select	NP_653302.2:p.Glu503Gln